ClinVar Miner

Submissions for variant NM_020975.6(RET):c.2802-4G>T (rs878855061)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000234020 SCV000290553 likely benign Multiple endocrine neoplasia, type 2 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000564506 SCV000664448 uncertain significance Hereditary cancer-predisposing syndrome 2019-07-14 criteria provided, single submitter clinical testing Insufficient evidence
Counsyl RCV000662545 SCV000785125 likely benign Multiple endocrine neoplasia, type 2a 2017-05-01 criteria provided, single submitter clinical testing

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